Z-1557-2015 Class II Terminated
Recall Details
- Product Type
- Devices
- Report Date
- May 6, 2015
- Initiation Date
- March 13, 2015
- Termination Date
- October 7, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 399
Product Description
Introduction Pack. A device inserted into an endotracheal tube to aid in the intubation procedure.
Reason for Recall
Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand Stylet catalog numbers 3910 and 3960 due to a potential patient safety risk involving a breach in the sterile packaging that may not be recognized prior to use.
Distribution Pattern
Worldwide Distribution. US Nationwide, Australia, Canada, Chile, Colombia, Dominican Republic, Ecuador, Egypt, Germany, Guatemala, Hong Kong, India, Israel, Italy, Japan, South Korea, Lebanon, Mexico, Netherlands, New Zealand, Panama, Peru, Poland, Russia, Slovenia, Turkey, United Kingdom, and Qatar.
Code Information
Catalog Number 3960